2017
DOI: 10.18203/2349-3291.ijcp20175542
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Spontaneous resolution of CCAM: a rare presentation

Abstract: Congenital cystic adenomatoid malformation (CCAM) is a rare developmental abnormality of lung occuring in 1-4/100000 live births. The mainstay of treatment is usually surgical excision as it can lead to recurrent pneumonias, abscess or malignancy. We here report a rare case of CCAM who presented at one year of age with right sided lung cysts and had favorable outcome as it resolved spontaneously.

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Cited by 1 publication
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“…With a lobectomy, the remaining lung could develop, thus, the total lung volume and its function will improve to normal levels [ 14 ]. The lobectomy procedure has a low rate of complications, and this intervention is expected to prevent recurrent lung infection and its transformation to malignancy [ 5 ]. From thorax CT-scan imaging, in our patient, the mediastinal structure was shown shifting to the right, causing a very severe respiratory acidosis for the patient due to the air trapping that led to carbon dioxide elevation.…”
Section: Discussionmentioning
confidence: 99%
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“…With a lobectomy, the remaining lung could develop, thus, the total lung volume and its function will improve to normal levels [ 14 ]. The lobectomy procedure has a low rate of complications, and this intervention is expected to prevent recurrent lung infection and its transformation to malignancy [ 5 ]. From thorax CT-scan imaging, in our patient, the mediastinal structure was shown shifting to the right, causing a very severe respiratory acidosis for the patient due to the air trapping that led to carbon dioxide elevation.…”
Section: Discussionmentioning
confidence: 99%
“…With lobectomy, the lung function will usually be resolved, resulting in normal total lung volume. Research showed CCAM could be resolved completely with only 4 % that needed further interventions [ 5 ].…”
Section: Introductionmentioning
confidence: 99%
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